Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 69315548 | HCID 69315548 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 69313037 | HCID 69313037 | 68.3% |
Reaction Steps
To the solution of 4-[N-[1-[N-(furan-2-ylcarbonyl)amino]cyclohexane carbonyl]amino]-1-[4-fluoro-2-(3,3-dimethylazetidin-2-one-1-yl)phenyl]piperidin-3-ol (0.5 g) obtained in Step 2 in 10 ml of dimethylsulfoxide, was added 0.5 ml of triethylamine. The reaction mixture was cooled to 0° C. Pyridine-SO3 complex (0.45 g) was added to the reaction mixture, which was then stirred for about 4 hours at room temperature. The reaction mixture was diluted with 20 ml of ethyl acetate and washed with brine. The resulting organic layer was dried and concentrated on sodium sulfate. The resulting residue was filtered and dried to give 340 mg of the titled compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07342027B2 |
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| Source dataset | uspto-grants-2008_03 |
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| ORD ID | ord-bbb18cbeacda4351aa10532997e6cf5a |
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| Source note | uspto-grants-2008_03 |
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